At a Glance
- Tasks: Support Oncology studies by monitoring sites and ensuring compliance with protocols.
- Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
- Benefits: Gain valuable experience, competitive salary, and opportunities for professional growth.
- Other info: Flexible travel required; dynamic environment with a focus on integrity.
- Why this job: Make a real difference in healthcare while working on innovative medical treatments.
- Qualifications: Life science degree or equivalent experience; independent monitoring skills required.
The predicted salary is between 30000 - 40000 £ per year.
IQVIA's Site Management (multi-sponsor) team are seeking a Clinical Research Associate to join us on our mission to help create a healthier world. The Clinical Research Associate will support Oncology studies and cover sites across the UK.
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
- Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.
- Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
- Collaborate and liaise with study team members for project execution support as appropriate.
- Experience of independent on-site monitoring of Oncology therapeutic area for unblinded studies.
- Life science degree educated or equivalent industry experience.
- Flexibility to travel to sites as required.
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law.
Research Administrator - Research and Development in Chesterfield employer: IQVIA
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation in the field of clinical research. Our commitment to employee growth is evident through comprehensive training programmes and opportunities for advancement, particularly in our dedicated Oncology studies across the UK. Join us in our mission to create a healthier world, where your contributions will be valued and impactful.
